A versatile method for tuning the chemistry and size of nanoscopic features by living free radical polymerization

被引:149
作者
von Werne, TA
Germack, DS
Hagberg, EC
Sheares, VV
Hawker, CJ
Carter, KR
机构
[1] IBM Corp, Almaden Res Ctr, Ctr Polymer Interfaces & Macromol Assemblies, San Jose, CA 95120 USA
[2] Iowa State Univ, Dept Chem, Ames, IA 50011 USA
关键词
D O I
10.1021/ja028866n
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A novel approach is presented for manipulating the size and chemistry of nanoscopic features using a combination of contact molding and living free radical polymerization. In this approach a highly cross-linked photopolymer, based on a methacrylate/acrylate mixture, was patterned into submicrometer-sized features on a silicon wafer using a contact-molding technique. A critical component of the monomer mixture was the incorporation of an initiator containing monomer into the network structure, which provides sites for functional group amplification. Features ranging in size from 5 mum to <60 nm were accurately replicated by this process and living free radical polymerizations, both atom transfer radical and nitroxide-mediated polymerization (NMP), could be conducted from these initiating sites to yield polymer brushes which represent a grafted layer of linear chains attached to the original network polymer. Grafts consisting of polystyrene, poly(methyl methacrylate), and poly(2-hydroxyethyl)methacrylate were grown with controlled thicknesses ranging from 10 to 143 nm and graft molecular weights of between 18000 to 290000 amu. As a result of this secondary graft process, feature sizes could be tuned from the original 100 nm down to 20 nm, and the surface chemistry varied from hydrophilic to hydrophobic starting from the same initial master pattern. The thin films and patterned features were characterized by contact angle, ellipsometry, optical, and atomic force microscopies.
引用
收藏
页码:3831 / 3838
页数:8
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